Term Name:	autosomal dominant intellectual developmental disorder 68
Synonyms:
Definition:	An autosomal dominant intellectual developmental disorder characterized by developmental delay/intellectual disability, primary autosomal recessive microcephaly, poor growth, feeding difficulties, and dysmorphic features that has_material_basis_in heterozygous mutation in the KMT2B gene on chromosome 19q13.
Ontology:	Human Disease [DOID:0061041]   ( DOID:0061041 )